Canonical Allele Identifier: CA411376824
Gene: CACNG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.36960709A>T (hg19) chr22:g.36564662A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36564662A>T , CM000684.2:g.36564662A>T GRCh38
NC_000022.10:g.36960709A>T , CM000684.1:g.36960709A>T GRCh37
NC_000022.9:g.35290655A>T NCBI36
NG_031861.1:g.142982T>A
NG_031861.2:g.143197T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300105.7:c.661T>A MANE Select ENSP00000300105.6:p.Ser221Thr
ENST00000300105.6:c.661T>A ENSP00000300105.6:p.Ser221Thr
NM_006078.3:c.661T>A NP_006069.1:p.Ser221Thr
NM_006078.4:c.661T>A NP_006069.1:p.Ser221Thr
XM_017028531.2:c.403T>A XP_016884020.1:p.Ser135Thr
NM_001379051.1:c.592T>A NP_001365980.1:p.Ser198Thr
NM_006078.5:c.661T>A MANE Select NP_006069.1:p.Ser221Thr
NR_166440.1:n.2027T>A
Search 100 bp 5'
Search 100 bp 3'